Primary Device ID | 10721902187046 |
NIH Device Record Key | 7496329f-fd4c-4684-9d93-dee883916532 |
Commercial Distribution Discontinuation | 2018-06-21 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 5846A |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Length | 6 Feet |
Length | 6 Feet |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Storage Environment Temperature | Between -40 Degrees Fahrenheit and 158 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00721902187049 [Primary] |
GS1 | 10721902187046 [Package] Contains: 00721902187049 Package: PK [5 Units] Discontinued: 2018-06-21 Not in Commercial Distribution |
LWP | Implantable pulse generator, pacemaker (non-CRT) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2014-09-23 |
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